Works matching DE "SULFONYL chlorides"
Results: 233
Switchable Deep Eutectic Solvents for Sustainable Sulfonamide Synthesis.
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- Chemistry - A European Journal, 2024, v. 30, n. 55, p. 1, doi. 10.1002/chem.202402293
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Preparation of chlorosulfonated polyethylene by liquid-solid method and comparison with industrial products.
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- Journal of Polymer Research, 2018, v. 25, n. 11, p. 1, doi. 10.1007/s10965-018-1624-1
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Synthesis and characterization of polyaniline co-doped with nitric acid and dodecyl benzene sulfonic acid.
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- Journal of Polymer Research, 2016, v. 24, n. 1, p. 1, doi. 10.1007/s10965-016-1175-2
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Synthetic Transformations of Higher Terpenoids. 44<sup>#</sup>. Synthesis of New Derivatives of 18-Nor-4-Amino-8(17),13,14-Labdatriene and Evaluation of Their Cytotoxicity for MCF7, HepG2, and HeLa Tumor Cell Lines.
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- Chemistry of Natural Compounds, 2024, v. 60, n. 2, p. 252, doi. 10.1007/s10600-024-04299-2
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Reaction of 5-Hydroxymethyl-6-Methyluracil with Toluenesulfonyl Chloride or Methanesulfonyl Chloride and Tertiary Amines.
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- Chemistry of Natural Compounds, 2017, v. 53, n. 4, p. 714, doi. 10.1007/s10600-017-2097-x
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Disulfonamide Piperazine Derivatives: Synthesis, Characterization, Crystal Structures Studies, and Evaluation of Cell Proliferation Activity.
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- Russian Journal of General Chemistry, 2024, v. 94, n. 8, p. 2167, doi. 10.1134/S1070363224080267
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Synthesis and Antitumor Activity of 5-Phenyl-1,3-thiazole-4-sulfonamide Derivatives.
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- Russian Journal of General Chemistry, 2022, v. 92, n. 2, p. 174, doi. 10.1134/S1070363222020062
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Synthesis, Molecular Docking, Analgesic, and Anti-Inflammatory Activities of New 1,2,4-Oxadiazolo-Sulfonamides.
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- Russian Journal of General Chemistry, 2018, v. 88, n. 4, p. 804, doi. 10.1134/S1070363218040278
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Preparation and properties of 2-methyl-4-tosyl-1,3-thiazole-5-sulfonyl chloride.
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- Russian Journal of General Chemistry, 2014, v. 84, n. 11, p. 2102, doi. 10.1134/S1070363214110103
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Interaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with amidines.
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- Russian Journal of General Chemistry, 2013, v. 83, n. 7, p. 1402, doi. 10.1134/S1070363213070165
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Synthesis of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides and N-substituted sulfonamides.
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- Russian Journal of General Chemistry, 2012, v. 82, n. 11, p. 1855, doi. 10.1134/S1070363212110229
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Phosphorus halides complexes with 4-dimethylaminopyridine and N-methylimidazole.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 5, p. 911, doi. 10.1134/S1070363209050089
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α-Hydroxy- and (α-acyloxyimino)benzylphosphonates.
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- Russian Journal of General Chemistry, 2009, v. 79, n. 2, p. 195, doi. 10.1134/S1070363209020054
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Homolytic Decomposition of Sulfonyl Chlorides.
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- Doklady Chemistry, 2018, v. 480, n. 1, p. 93, doi. 10.1134/S0012500818050063
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Synthesis and inhibitive characteristic of two acryloyl chloride derivatives towards the corrosion of API 5L X52 carbon steel in hydrochloric acid medium.
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- Zeitschrift für Physikalische Chemie, 2022, v. 236, n. 4, p. 535, doi. 10.1515/zpch-2021-3170
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Progression to insulin for patients with diabetes mellitus on dual oral antidiabetic therapy using the US Department of Defense Database.
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- Diabetes, Obesity & Metabolism, 2013, v. 15, n. 10, p. 901, doi. 10.1111/dom.12103
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Nanocomposite Anion Exchange Membranes with a Conductive Semi-Interpenetrating Silica Network.
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- Membranes, 2021, v. 11, n. 4, p. 260, doi. 10.3390/membranes11040260
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Oxidative cleavage and ammoxidation of organosulfur compounds via synergistic Co-Nx sites and Co nanoparticles catalysis.
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- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-38614-2
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Halide perovskites as disposable epitaxial templates for the phase-selective synthesis of lead sulfochloride nanocrystals.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31699-1
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One-pot synthesis of sulfonylhydrazones from sulfonyl chloride, hydrazine hydrate and vinyl azide in water.
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- Journal of the Iranian Chemical Society, 2021, v. 18, n. 10, p. 2713, doi. 10.1007/s13738-021-02226-8
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Ir-catalyzed C-S coupling of quinones with sulfonyl chloride.
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- Journal of the Iranian Chemical Society, 2016, v. 13, n. 10, p. 1797, doi. 10.1007/s13738-016-0897-8
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CALIBRATION OF A PASSIVE SAMPLING DEVICE FOR TIME-INTEGRATED SAMPLING OF HYDROPHILIC HERBICIDES IN AQUATIC ENVIRONMENTS.
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- Environmental Toxicology & Chemistry, 2007, v. 26, n. 3, p. 435, doi. 10.1897/06-401R.1
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Convenient synthesis of sulfonyl azides using PEG-400 as an efficient and eco-friendly reaction medium.
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- Green Chemistry Letters & Reviews, 2013, v. 6, n. 3, p. 222, doi. 10.1080/17518253.2012.750688
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Investigation of Chemoselective Reaction of 2-Amino-8-hydroxyquinoline with Arylsulfonylchloride Derivatives.
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- Synthetic Communications, 2009, v. 39, n. 8, p. 1378, doi. 10.1080/00397910802527730
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Asymmetric Addition of Diethylzinc to Ketones promoted by Tartaric Acid Derivatives.
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- Synthetic Communications, 2008, v. 38, n. 14, p. 2374, doi. 10.1080/00397910802139304
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Synthesis, Anticancer and Antitubercular Properties of New Chalcones and Their Nitrogen-Containing Five-Membered Heterocyclic Hybrids Bearing Sulfonamide Moiety.
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- International Journal of Molecular Sciences, 2022, v. 23, n. 20, p. 12589, doi. 10.3390/ijms232012589
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Calculated Third Order Rate Constants for Interpreting the Mechanisms of Hydrolyses of Chloroformates, Carboxylic Acid Halides, Sulfonyl Chlorides and Phosphorochloridates.
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- International Journal of Molecular Sciences, 2015, v. 16, n. 5, p. 10601, doi. 10.3390/ijms160510601
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Synthesis, characterization, and properties of a novel polyhedral oligomeric octamethyldiphenylsulfonylsilsesquioxane.
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- Journal of Materials Science, 2015, v. 50, n. 2, p. 697, doi. 10.1007/s10853-014-8629-x
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Chemoselective Reactions of Functionalized Sulfonyl Halides.
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- Chemical Record, 2024, v. 24, n. 2, p. 1, doi. 10.1002/tcr.202300256
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2-Amino-5-sulfanyl-1,3,4-thiadiazoles: a novel series of anti-inflammatory and analgesic agents.
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- Pharmaceutical Chemistry Journal, 2009, v. 43, n. 1, p. 19, doi. 10.1007/s11094-009-0236-9
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Synthesis, characterization and electrochemical properties of some biologically important indole-based-sulfonamide derivatives.
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- BMC Chemistry, 2020, v. 14, n. 1, p. 1, doi. 10.1186/s13065-020-00691-5
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Nucleophilic Substitution in 6-Chloro-2-(2-cyano-phenoxy)quinoxalines and Antibacterial Activity of Phenoxychloroquinoxaline Derivatives.
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- Russian Journal of Organic Chemistry, 2021, v. 57, n. 4, p. 647, doi. 10.1134/S1070428021040217
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Synthesis of New Sulfonamides Based on β-Pinene.
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- Russian Journal of Organic Chemistry, 2020, v. 56, n. 3, p. 405, doi. 10.1134/S1070428020030070
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Synthesis and Oxidation of Myrtanethiol and Its Functional Derivatives with Chlorine Dioxide.
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- Russian Journal of Organic Chemistry, 2019, v. 55, n. 10, p. 1469, doi. 10.1134/S107042801910004X
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Synthesis of 2,5-dihydroimidazo[4,5- e][1,2,3]thiadiazine 1,1-dioxides-Derivatives of a novel heterocyclic system.
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- Russian Journal of Organic Chemistry, 2017, v. 53, n. 12, p. 1890, doi. 10.1134/S107042801712020X
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New synthesis of 3,5-diaryl-1,2,4-oxadiazoles containing a sulfonyl chloride or sulfonamide group.
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- Russian Journal of Organic Chemistry, 2015, v. 51, n. 7, p. 988, doi. 10.1134/S1070428015070167
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N-Propargyltrifluoromethanesulfonamide.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 5, p. 747, doi. 10.1134/S1070428014050212
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2,2-Bis(methoxy- and ethoxy-NNO-azoxy)propane-1,3-diol sulfonates.
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- Russian Journal of Organic Chemistry, 2014, v. 50, n. 5, p. 631, doi. 10.1134/S1070428014050030
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N-allenyl- N-benzyltrifl uoromethanesulfonamide.
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- Russian Journal of Organic Chemistry, 2013, v. 49, n. 8, p. 1112, doi. 10.1134/S1070428013080034
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Optimization of the synthesis of phenanthrene-2- and -3-sulfonyl chlorides.
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- Russian Journal of Organic Chemistry, 2012, v. 48, n. 4, p. 547, doi. 10.1134/S1070428012040148
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Intramolecular electrophilic cyclization of functional derivatives of unsaturated Compounds: I. Synthesis of 5-arylsulfanyl-6-phenylpiperidin-2-ones from cinnamylacetamides and arylsulfenyl chlorides.
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- Russian Journal of Organic Chemistry, 2011, v. 47, n. 8, p. 1146, doi. 10.1134/S1070428011080057
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New synthesis of alkane- and arylsulfonyl chlorides by oxidation of thiols and disulfides with chlorine dioxide.
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- Russian Journal of Organic Chemistry, 2011, v. 47, n. 8, p. 1249, doi. 10.1134/S1070428011080239
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Regio- and stereoselective addition of methane- and bromomethanesulfonyl bromides to 1-phenylthiotricyclo[4.1.0.0<sup>2,7</sup>]heptane.
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- Russian Journal of Organic Chemistry, 2010, v. 46, n. 5, p. 624, doi. 10.1134/S1070428010050027
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Synthesis of sufamides of indole series.
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- Russian Journal of Organic Chemistry, 2009, v. 45, n. 11, p. 1675, doi. 10.1134/S1070428009110153
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Hydroxyalkylammonium salts of organylsulfanyl(sulfonyl)acetic acids—New stimulators of biological processes.
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- Russian Journal of Organic Chemistry, 2008, v. 44, n. 10, p. 1478, doi. 10.1134/S1070428008100126
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Cross-linked chitosan aerogel modified with Pd(II)/phthalocyanine: Synthesis, characterization, and catalytic application.
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- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-50021-6
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Halide perovskites as disposable epitaxial templates for the phase-selective synthesis of lead sulfochloride nanocrystals.
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- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-31699-1
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- Publication type:
- Article
N-Sulfonated derivatives of (2-furoyl)piperazine: Promising antibacterial agents with mild cytotoxicity.
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- Pakistan Journal of Pharmaceutical Sciences, 2022, v. 35, n. 2, p. 579, doi. 10.36721/PJPS.2022.35.2.REG.579-585.1
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Synthesis of some N-sulfonated derivatives of 1-[(E)-3-phenyl-2- propenyl]piperazine as suitable antibacterial agents.
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- Pakistan Journal of Pharmaceutical Sciences, 2020, v. 33, n. 4, p. 1609, doi. 10.36721/PJPS.2020.33.4.REG.1609-1616.1
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Synthesis, characterization and biological screening of sulfonamides derived form 2-phenylethylamine.
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- Pakistan Journal of Pharmaceutical Sciences, 2012, v. 25, n. 4, p. 809
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- Article